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Updated: May 26, 2026

Ultrafast Lignin Extraction from Unusual Mediterranean Lignocellulosic Residues
Published on: March 9, 2021
A new lignan glycoside from Juniperus rigida.
Kyeong Wan Woo1, Sang Un Choi, Jong Cheol Park
1Natural Products Laboratory, School of Pharmacy, Sungkyunkwan University, Suwon, 440-746, Korea.
A new lignan glycoside, juniperigiside, was isolated from Juniperus rigida. Several lignans and diterpenes were identified, with some showing significant cytotoxicity against human cancer cell lines in vitro.
Area of Science:
- Phytochemistry
- Natural Products Chemistry
- Pharmacology
Background:
- Juniperus rigida is a plant species with potential medicinal properties.
- Natural products are a rich source of bioactive compounds.
- Lignans and diterpenes are classes of natural products known for diverse biological activities.
Purpose of the Study:
- To isolate and identify chemical constituents from Juniperus rigida stems and leaves.
- To evaluate the cytotoxic activity of isolated compounds against human tumor cell lines.
- To discover new bioactive compounds from this plant species.
Main Methods:
- Extraction of plant material using methanol and subsequent fractionation.
- Isolation of compounds using chromatographic techniques.
- Structure elucidation using 1D- and 2D-NMR spectroscopy, CD analysis, and comparison with literature data.
- Cytotoxicity assessment using the Sulforhodamin B bioassay.
Main Results:
- A new lignan glycoside, juniperigiside (1), was isolated and characterized.
- Five known lignans (2-6) and five known labdane diterpenes (7-11) were identified.
- Compounds 5 and 6 were reported for the first time in the Juniperus genus.
- Compounds 3 (desoxypodophyllotoxin), 4 (savinin), 7 (trans-communic acid), and 8 (13-epi-torulosal) exhibited considerable cytotoxicity against tested cancer cell lines.
Conclusions:
- Juniperus rigida is a source of diverse lignans and diterpenes, including novel compounds.
- Several isolated lignans and diterpenes possess significant in vitro cytotoxic activity against human tumor cells.
- The findings support further investigation of these compounds for potential anticancer drug development.
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